MYLANTA ORIGINAL oral liquid bottle (reformulation 2) Úc - Tiếng Anh - Department of Health (Therapeutic Goods Administration)

mylanta original oral liquid bottle (reformulation 2)

johnson & johnson pacific pty ltd - simethicone, quantity: 4 mg/ml; aluminium hydroxide, quantity: 40 mg/ml; magnesium hydroxide, quantity: 40 mg/ml - oral liquid, suspension - excipient ingredients: ethyl hydroxybenzoate; xanthan gum; xylitol; purified water; sorbitol solution (70 per cent) (non-crystallising); butyl hydroxybenzoate; ethanol; propyl hydroxybenzoate; acesulfame potassium; flavour; simethicone; sorbic acid; dimeticone 100; peg-4 stearate; glyceryl distearate; peg-3 distearate; peg-20 stearate; hydrogen peroxide - relief from indigestion, heartburn, upset stomach, flatulence and wind pain.

MYLANTA P ANTACID oral liquid bottle (reformulation) Úc - Tiếng Anh - Department of Health (Therapeutic Goods Administration)

mylanta p antacid oral liquid bottle (reformulation)

johnson & johnson pacific pty ltd - simethicone, quantity: 4 mg/ml; aluminium hydroxide, quantity: 40 mg/ml; magnesium hydroxide, quantity: 40 mg/ml - oral liquid, suspension - excipient ingredients: butyl hydroxybenzoate; sorbitol solution (70 per cent) (non-crystallising); xylitol; purified water; propyl hydroxybenzoate; xanthan gum; acesulfame potassium; ethyl hydroxybenzoate; ethanol; flavour; simethicone; sorbic acid; dimeticone 100; peg-4 stearate; glyceryl distearate; peg-3 distearate; peg-20 stearate; hydrogen peroxide - relief from indigestion, heartburn, upset stomach, flatulence and wind pain.

GELUSIL oral liquid bottle (reformulation 2) Úc - Tiếng Anh - Department of Health (Therapeutic Goods Administration)

gelusil oral liquid bottle (reformulation 2)

johnson & johnson pacific pty ltd - aluminium hydroxide,aluminium hydroxide hydrate,magnesium hydroxide,simethicone -

MYLANTA 2go ANTACID ORIGINAL chewable tablet (reformulation) blister pack Úc - Tiếng Anh - Department of Health (Therapeutic Goods Administration)

mylanta 2go antacid original chewable tablet (reformulation) blister pack

johnson & johnson pacific pty ltd - simethicone, quantity: 20 mg; magnesium hydroxide, quantity: 200 mg; aluminium hydroxide, quantity: 200 mg - tablet, chewable - excipient ingredients: mannitol; spearmint oil; purified water; magnesium stearate; maize starch; sucrose; silicon dioxide; dimeticone 1000; dimeticonol; flavour - fast relief from upset stomach, flatulence, wind pain, gastric hyperacidity, indigestion, heartburn and oesophageal reflux.

MYLANTA 2go ANTACID DOUBLE STRENGTH chewable tablet (reformulation) blister pack Úc - Tiếng Anh - Department of Health (Therapeutic Goods Administration)

mylanta 2go antacid double strength chewable tablet (reformulation) blister pack

johnson & johnson pacific pty ltd - simethicone, quantity: 40 mg; magnesium hydroxide, quantity: 400 mg; aluminium hydroxide, quantity: 400 mg - tablet, chewable - excipient ingredients: mannitol; magnesium stearate; purified water; spearmint oil; silicon dioxide; dimeticone 1000; dimeticonol; flavour; maize starch; sucrose - fast relief from upset stomach, flatulence, wind pain, gastric hyperacidity, indigestion, heartburn and oesophageal reflux.

GELUSIL tablets (reformulation) blister pack Úc - Tiếng Anh - Department of Health (Therapeutic Goods Administration)

gelusil tablets (reformulation) blister pack

johnson & johnson pacific pty ltd - aluminium hydroxide,magnesium hydroxide,simethicone -

CHEMISTS' OWN DECONGESTANT NASAL SPRAY (REFORMULATION) oxymetazoline hydrochloride 0.5mg/mL metered dose pump actuated aerosol and refill bottle Úc - Tiếng Anh - Department of Health (Therapeutic Goods Administration)

chemists' own decongestant nasal spray (reformulation) oxymetazoline hydrochloride 0.5mg/ml metered dose pump actuated aerosol and refill bottle

arrotex pharmaceuticals pty ltd - oxymetazoline hydrochloride, quantity: 0.5 mg/ml - spray - excipient ingredients: benzalkonium chloride; monobasic sodium phosphate; purified water; propylene glycol; cineole; dibasic sodium phosphate heptahydrate; disodium edetate; menthol - provides temporary and symptomatic relief of nasal and sinus congestion caused by the common cold, sinusitis, hayfever, or other upper respiratory allergies.

K.P. 24 MEDICATED FOAM malathion 1% application bottle (reformulation) Úc - Tiếng Anh - Department of Health (Therapeutic Goods Administration)

k.p. 24 medicated foam malathion 1% application bottle (reformulation)

pharmacare laboratories pty ltd - malathion, quantity: 13 mg/g - application - excipient ingredients: purified water; butylated hydroxytoluene; laureth-2; citric acid; cocamide dea; sodium citrate dihydrate; trolamine lauril sulfate; fragrance (perfume); isopropyl 4-hydroxybenzoate; isobutyl hydroxybenzoate; butyl hydroxybenzoate; phenoxyethanol - for the treatment of head lice and their eggs.

K.P. 24 MEDICATED LOTION malathion 0.5% topical solution bottle (reformulation) Úc - Tiếng Anh - Department of Health (Therapeutic Goods Administration)

k.p. 24 medicated lotion malathion 0.5% topical solution bottle (reformulation)

pharmacare laboratories pty ltd - malathion, quantity: 5 mg/g - solution - excipient ingredients: isopropyl myristate; fragrance (perfume) - for the treatment of head lice and their eggs.

NUROFEN PLUS tablet blister pack (reformulation) Úc - Tiếng Anh - Department of Health (Therapeutic Goods Administration)

nurofen plus tablet blister pack (reformulation)

reckitt benckiser pty ltd - ibuprofen, quantity: 200 mg; codeine phosphate hemihydrate, quantity: 12.8 mg - tablet, film coated - excipient ingredients: hypromellose; sodium starch glycollate; microcrystalline cellulose; purified talc; pregelatinised maize starch; titanium dioxide; purified water; industrial methylated spirit - for the temporary relief of acute moderate pain and inflammation in patients over the age of 12 years ( see also contraindications and paediatric use)